NDCFind

Betaxolol 42806-0039

Product NDC

42806-0039
Manufacturer
Epic Pharma Llc
Dosage Form
Tablet, Film Coated
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
July 20, 2010
Listing Expires
December 31, 2026
Application
ANDA075541
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Active Ingredients

IngredientStrength
Betaxolol Hydrochloride20 mg/1

Drug Class

Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]

Packaging Options(2)

100 TABLET, FILM COATED in 1 BOTTLE (42806-039-01)

1000 TABLET, FILM COATED in 1 BOTTLE (42806-039-10)